Constructing efficient bacterial cell factories to enable one‐carbon utilization based on quantitative biology: A review

Author:

Song Yazhen1,Feng Chenxi1,Zhou Difei1,Ma Zengxin1,He Lian2,Zhang Cong1,Yu Guihong1,Zhao Yan1,Yang Song13,Xing Xinhui456

Affiliation:

1. School of Life Sciences Shandong Province Key Laboratory of Applied Mycology, and Qingdao International Center on Microbes Utilizing Biogas Qingdao Agricultural University Qingdao China

2. Department of Chemical Engineering University of Washington Seattle Washington USA

3. Key Laboratory of Systems Bioengineering Ministry of Education Tianjin University Tianjin China

4. Key Laboratory of Industrial Biocatalysis Ministry of Education Department of Chemical Engineering Tsinghua University Beijing China

5. Center for Synthetic and Systems Biology Tsinghua University Beijing China

6. Institute of Biopharmaceutical and Health Engineering Tsinghua Shenzhen International Graduate School, and Institute of Biomedical Health Technology and Engineering Shenzhen Bay Laboratory Shenzhen China

Abstract

AbstractDeveloping methylotrophic cell factories that can efficiently catalyze organic one‐carbon (C1) feedstocks derived from electrocatalytic reduction of carbon dioxide into bio‐based chemicals and biofuels is of strategic significance for building a carbon‐neutral, sustainable economic and industrial system. With the rapid advancement of RNA sequencing technology and mass spectrometer analysis, researchers have used these quantitative microbiology methods extensively, especially isotope‐based metabolic flux analysis, to study the metabolic processes initiating from C1 feedstocks in natural C1‐utilizing bacteria and synthetic C1 bacteria. This paper reviews the use of advanced quantitative analysis in recent years to understand the metabolic network and basic principles in the metabolism of natural C1‐utilizing bacteria grown on methane, methanol, or formate. The acquired knowledge serves as a guide to rewire the central methylotrophic metabolism of natural C1‐utilizing bacteria to improve the carbon conversion efficiency, and to engineer non‐C1‐utilizing bacteria into synthetic strains that can use C1 feedstocks as the sole carbon and energy source. These progresses ultimately enhance the design and construction of highly efficient C1‐based cell factories to synthesize diverse high value‐added products. The integration of quantitative biology and synthetic biology will advance the iterative cycle of understand–design–build–testing–learning to enhance C1‐based biomanufacturing in the future.

Publisher

Wiley

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